Publications by authors named "Roman Solc"

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New Insights Into Changes in the DNA Methylation Pattern of the SHOX Gene in Patients With Léri-Weill Dyschondrosteosis.
Valeriia Kopytko, Katerina Hirschfeldova, Pavlina Capkova, Roman Solc

Am J Med Genet A· October 2025

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Role of cryptic rearrangements of human chromosomes in the aetiology of schizophrenia.
Livia Jurisova, Roman Solc

J Genet· June 2023

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Inversions on human chromosomes.
Klara Kosuthova, Roman Solc

Am J Med Genet A· March 2023

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Epigenetic Regulation of Circadian Rhythm and Its Possible Role in Diabetes Mellitus.
Michael Hudec, Pavlina Dankova, Roman Solc, Nardjas Bettazova, Marie Cerna

Int J Mol Sci· April 2020

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Comparison of SHOX and associated elements duplications distribution between patients (Lėri-Weill dyschondrosteosis/idiopathic short stature) and population sample.
Katerina Hirschfeldova, Roman Solc

Gene· September 2017

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Mutation analysis of TRPS1 gene including core promoter, 5'UTR, and 3'UTR regulatory sequences with insight into their organization.
Roman Solc, Michaela Klugerova, Josef Vcelak, Alice Baxova, Miloslav Kuklik

Clin Chim Acta· January 2017

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Analysis of common SHOX gene sequence variants and ~4.9-kb PAR1 deletion in ISS patients.
Roman Solc, Katerina Hirschfeldova, Vera Kebrdlova, Alice Baxova

J Genet· August 2014

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Cryptic chromosomal rearrangements in children with idiopathic mental retardation in the Czech population.
Katerina Hirschfeldova, Alice Baxova, Vera Kebrdlova, Roman Solc, Romana Mihalova

Genet Test Mol Biomarkers· September 2011

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